A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17072256



Internal ID21490174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:91055626..91055946hg38UCSC Ensembl
chr10:92815383..92815703hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg38321
hg19321
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5587872
Supporting Variants
SamplesNA19238
Known GenesLINC00502
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17072256
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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